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Inherited cancer susceptibility gene mutations among patients with appendix cancer

Oncology
Research

Speakers:
Andreana Holowatyi

Conference:
CGA-IGC 2022

Friday, Nov 11, 2022 2:30pm – 4:15pm
Disparities in the uptake of cascade genetic testing among family members of mutation-positive Lynch and HBOC syndrome patients

Oncology
Research

Speakers:
Elia Namey

Conference:
CGA-IGC 2022

Friday, Nov 11, 2022 2:30pm – 4:15pm

Collaborators:

University of Pittsburgh Medical Center (UPMC)
Utility of RNA testing in individuals at increased risk for hereditary or familial pancreatic cancer

Oncology
Research

Speakers:
Beth Dudley

Conference:
CGA-IGC 2022

Friday, Nov 11, 2022 2:30pm – 4:15pm

Collaborators:

University of Pittsburgh Medical Center (UPMC)

Abstract
Bringing genetics into your practice: Talk to your office admin

Clinician

Speakers:
Jordan Karlitz

Conference:
ACG 2022

Monday, Oct 24, 2022 10:30am – 11:30am
Mutation spectrum and rates of variants of uncertain significance among African American males undergoing prostate cancer germline testing: Need for equity in genetic testing

Oncology

Speakers:
Veda N. Giri, Rebecca Hartman, Mary Pritzlaff, Scott Keith

Conference:
ASCO 2022

Friday, Jun 3, 2022 12:00pm – 12:00pm

Abstract
Application of RNA sequencing evidence improves equity in variant interpretation

Clinical Genomics

Speakers:
Carolyn Horton, Lily Hoang, Holly LaDuca, Min-Tzu Lo, Heather Zimmermann, Ashley Cass, Blair Conner, Nelly Abualkheir, Jessica Grzybowski, Kate Durda, Robert Pilarski, Elizabeth Chao, Rachid Karam

Conference:
ACMG 2022

Tuesday, Mar 22, 2022 12:00am – 12:00pm

Abstract
Expanding access to genetic services at community clinics using a virtual assistant

CARE Marketing Resources

Speakers:
Michelle Jackson, Cassie Garcia, Lily Hoang, Cara Yobbi, Rebekah Krukenberg, Jennifer Moore, Sandra Jenkinson, Holly LaDuca, Sarah Campian, Kory Jasperson

Conference:
NSGC 2021

Saturday, Sep 25, 2021 10:30am – 12:00pm

Collaborators:

Community Health Network

Abstract
Implementation of routine genetic screening in a rural gastrointestinal clinic leads to the identification of inherited gastrointestinal disorders and other cancer risks in 20% of patients tested

Oncology

Speakers:
Howard P. Monsour, Carrie Milliard, Frederick Oriti, Cynthia Wade, Nicole Jennings, Michelle Stegenga, Linda L. Heflin, Paul Schmidt, Megan Week, Russell Peterson, Rachel Bluebond, Lily Hoang, Holly Laduca

Conference:
DDW 2022

Friday, May 21, 2021 12:00pm – 12:00pm

Abstract
The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

Oncology

Speakers:
Marcy Richardson, Chunling Hu, Kun Y. Lee, Holly LaDuca, Kelly Fulk, Kate M. Durda, Ashley M. Deckman, David E. Goldgar, Rohan Gnanaolivu, Steven N. Hart, Eric C. Polley, Elizabeth Chao, Tina Pesaran, Fergus J. Couch

Conference:
ACMG 2021

Tuesday, Apr 13, 2021 12:00am – 12:00pm

Collaborators:

Mayo Clinic
University of Utah

Abstract
Pathogenic duplications in tumor suppressor genes cause aberrant mRNA splicing

Oncology

Speakers:
Blair R. Conner, Marcy Richardson, Terra Brannan, Felicia Hernandez, Noriko Yokoyama, Tyler Landrith, Tamara McBride, Tina Pesaran, Rachid Karam

Conference:
ACMG 2021

Tuesday, Apr 13, 2021 12:00am – 12:00pm

Abstract

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Inherited cancer susceptibility gene mutations among patients with appendix cancer

Disparities in the uptake of cascade genetic testing among family members of mutation-positive Lynch and HBOC syndrome patients

Utility of RNA testing in individuals at increased risk for hereditary or familial pancreatic cancer

Bringing genetics into your practice: Talk to your office admin

Mutation spectrum and rates of variants of uncertain significance among African American males undergoing prostate cancer germline testing: Need for equity in genetic testing

Application of RNA sequencing evidence improves equity in variant interpretation

Expanding access to genetic services at community clinics using a virtual assistant

Implementation of routine genetic screening in a rural gastrointestinal clinic leads to the identification of inherited gastrointestinal disorders and other cancer risks in 20% of patients tested

The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

Pathogenic duplications in tumor suppressor genes cause aberrant mRNA splicing

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